US20080044732A1 - Nanostructured Electrode for a Microbattery - Google Patents

Nanostructured Electrode for a Microbattery Download PDF

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US20080044732A1
US20080044732A1 US11/793,893 US79389305A US2008044732A1 US 20080044732 A1 US20080044732 A1 US 20080044732A1 US 79389305 A US79389305 A US 79389305A US 2008044732 A1 US2008044732 A1 US 2008044732A1
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electrode
electrolyte
anode
lithium
components
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Raphael Salot
Frederic Gaillard
Emmanuelle Rouviere
Steve Martin
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Commissariat a lEnergie Atomique et aux Energies Alternatives CEA
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0402—Methods of deposition of the material
    • H01M4/0421—Methods of deposition of the material involving vapour deposition
    • H01M4/0428—Chemical vapour deposition
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562—Solid materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H01M10/0585—Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H01M4/0402—Methods of deposition of the material
    • H01M4/0421—Methods of deposition of the material involving vapour deposition
    • H01M4/0423—Physical vapour deposition
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/134—Electrodes based on metals, Si or alloys
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139—Processes of manufacture
    • H01M4/1393—Processes of manufacture of electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139—Processes of manufacture
    • H01M4/1395—Processes of manufacture of electrodes based on metals, Si or alloys
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00—Primary cells; Manufacture thereof
    • H01M6/40—Printed batteries, e.g. thin film batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0068—Solid electrolytes inorganic
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0088—Composites
    • H01M2300/0094—Composites in the form of layered products, e.g. coatings
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the invention relates to the field of power storage devices, and mainly of microbatteries made in thin films by vacuum deposition methods.
  • the invention relates to an electrode for a battery, notably a lithium battery, the structure of which is defined so as to optimize reliability of power storage.
  • microbatteries which are particularly used, so-called ⁇ fully solid>>batteries, are in the form of films: all the components of the microbattery, i.e., the current collectors, the positive and negative electrodes, the electrolyte and even the encapsulation, are thin layers, obtained by deposition, mainly by physical vapor deposition (PVD) or chemical vapor deposition (CVD).
  • PVD physical vapor deposition
  • CVD chemical vapor deposition
  • the operating principle of such a battery is based on the insertion and removal, also called ⁇ disinsertion>>, of an alkaline metal ion or a proton into and from the positive electrode, and the deposition or extraction of this ion on and from the negative electrode.
  • the operating voltage of this type of battery is between 1 and 4 V, and the surface capacities are of the order of a few 10 ⁇ Ah/cm 2 to a few hundreds of ⁇ Ah/cm 2 .
  • Recharging a microbattery, i.e., transferring ions from the anode to the cathode is generally complete after a few minutes of charging.
  • Li + as a ion species for transporting the current: the Li + ion extracted from the cathode during the discharge of the battery will be deposited on the anode, and vice versa, it will be extracted from the anode in order to be inserted in the cathode during the charging.
  • the melting point of lithium 181° C.
  • the strong reactivity of lithium metal with regard to the ambient atmosphere is a penalty, even for the encapsulation.
  • Li + ion battery Li-ion battery
  • a cathode the material of which contains lithium.
  • insertion of the Li + ion causes swelling of the material which receives it: even the most performing materials used as insertion anodes, such as Si, lead to significant volume expansions (up to 400%).
  • the stresses generated by such a difference in volume strongly strain the superimposed layers, and in particular may cause deteriorations, or even cracks, of the juxtaposed electrolyte, which may create short-circuits making the battery inoperative.
  • anodeless battery also known as a Li-free battery: depositing of Li + from the cathode is directly carried out on a substrate, a so-called blocking substrate.
  • the protrusions generated by the deposition however are also the source of strong deformations and of potential breaking of the electrolyte.
  • the electrolyte be changed so as to make it in several portions, by inserting inside it fine layers of another material, also a lithium ion conductor, in order to limit possible diffusion of cracks right through the electrolyte layer (see for example U.S. Pat. No. 6,770,176).
  • Such a solution however results in multiplying the number of layers to be deposited (with at least two different targets for the electrolyte), which increases the cost of the manufacturing method, and may only degrade the ionic conductivity of the electrolyte.
  • the object of the invention is to overcome the problems of the state of the art as for the stability of the power storage and supply. More particularly, the invention recommends the use of a new family of electrodes, the architecture and design of which provide suppression of the stresses on the electrolyte during the charging and discharging of the microbattery.
  • the invention relates to a microbattery, an electrode of which is formed by independent electrode components, which thereby define gaps without any electrode between them, or empty spaces.
  • the empty space rate is larger than 50%, for example of the order of 80%.
  • the relevant electrode is mainly the anode, the cathode and the solid electrolyte then being in the form of material layers, deposited more or less uniformly.
  • the anode consists of protrusions extending and protruding from a current-collecting substrate.
  • the anode consists of carbon nanotubes or silicon nanowires.
  • the power storage device according to the invention may be encapsulated in order to insulate the ion exchanger components from the outside.
  • the invention relates to a nanowire or nanotube structure on a conducting substrate which may be used for making lithium batteries, as an electrode.
  • FIG. 1 schematically illustrates power storage according to the invention.
  • FIGS. 2A and 2B show a device according to the invention in the charged condition and in the discharged condition, respectively.
  • a power storage device usually comprises a substrate 12 , cathode 14 a and anode 14 b collectors (the latter may be integral with the substrate 12 ), a cathode 16 , an electrolyte 18 , and an anode 20 .
  • the microbattery 10 may be protected by an encapsulation layer 22 : the electrodes 16 , 20 , notably when they are in lithium, are indeed very reactive towards air, and it may be advantageous to also encapsulate the other components 14 , 18 .
  • the total thickness of the stack 14 , 16 , 18 , 20 is usually between 10 and 50 ⁇ m, advantageously of the order of 15 ⁇ m.
  • Such a microbattery 10 except for the anode 20 which will be described later on, may be made by any known technique, and in particular with different materials:
  • the current collectors 14 are metal and may for example be deposits based on Pt, Cr, Au, Ti.
  • the positive electrode 16 may notably consist of LiCoO 2 , LiNiO 2 , LiMn 2 O 4 , CuS, CuS 2 , WO y S z , TiO y S z , V 2 O 5 , deposited by a standard technique, with possible thermal annealing in order to increase crystallization and insertion capabilities (notably for lithiated oxides).
  • the electrolyte 18 which is a good ionic conductor and an electronic insulator, generally consists of a glassy material based on boron oxide, on lithium salts or oxides, in particular a lithium oxynitride.
  • the electrolyte is based on a phosphate, such as LiPON, or LiSiPON.
  • the anode 20 is however made according to an architecture with which any expansion in the direction perpendicular to the surface of the collector substrate 14 b and at the adjacent electrolyte surface 18 may be suppressed.
  • This advantage is obtained by means of an electrode 20 comprising electrode components 24 spaced apart from each other, and therefore an anode 20 comprising empty spaces 26 : during discharge of the cathode 16 , lithium ions will cause swelling of the anode components 24 , but the expansion is achieved in the residual empty space 26 . Consequently, the electrolyte 18 , held by the free ends of the anode components 24 , no longer undergoes any induced stress during charging and discharging.
  • this empty space also allows Li + ions which are not inserted in the anode, to be received and which are deposited as lithium metal.
  • the electrolyte 18 is not at all strained by the expansion because, contrary to a liquid or a gel, the electrolyte 18 does not fit into the residual empty space 26 .
  • the initially present empty space proportion 26 compensates the increase in volume related to the insertion of lithium in the components 24 .
  • This optimization is specific to each insertion material, but the empty space rate is usually larger than 50%, preferably larger than 80%.
  • FIG. 2A illustrates the charged condition of the battery 10 , in which the anode 20 does not comprise any Li + ions.
  • the lithium ions will be inserted into the anode components 24 causing them to swell, so that the residual empty space 26 decreases.
  • FIG. 2B shows that even in the totally discharged condition of the battery, as schematized in FIG. 2B , the overall volume of the anode layer 20 has not changed, only the empty space rate 26 has decreased, so that neither the electrolyte 18 nor the collector layer 14 b have undergone any stress.
  • the materials used for making the protrusions 24 are materials into which lithium may be inserted (a preferred empty space rate is shown between brackets): germanium (80%), silicon-germanium (80%), silver, tin (70%), . . . and especially silicon (80%) or carbon (50%).
  • nanostructures i.e., with sectional dimensions less than a few tens of nanometers, in particular nanotubes and nanowires, is recommended in obtaining optimal results for the expansion problems.
  • electrode components 24 as nanotubes
  • an additional advantage resides in the fact that with the growth of these nanotubes, it is possible to do without the photolithographic step, a very difficult step because of the required precision.
  • any technology with which structures of this type may be obtained, may be used such as full layer deposition followed by the definition of small patterns by photolithography.
  • deposition of nanotubes or nanofibers techniques are described for example in the documents of Sharma S and al.: ⁇ Diameter control of Ti-catalyzed silicon nanowires>>, J. Crystal Growth 2004; 267: pp. 613-618, or Tang H and al.: ⁇ High dispersion and electrocatalytic properties of platinum on well-aligned carbon nanotube arrays>>, Carbon 2004; 42: pp. 191-197.
  • the electrode components 24 may be randomly positioned forming a sponge type network.
  • the components of electrodes are in the form of protrusions 24 protruding from the surface of the collector substrate 14 b, in particular as a regular network, for example a square or hexagonal network.
  • the diameter of the protrusions 24 and the pitch of the network may be optimized in order to obtain the sought-after-empty space rate.
  • the obtained network may be regular, with notably protrusions 24 which all protrude from the base surface 14 b, according to an angle advantageously as close as possible to 90°.
  • the protrusions 24 may thus consist in a network of wires with a diameter from 5 to 50 nm, spaced apart by 50 to 100 nm with heights between 200 nm and 5 ⁇ m.
  • a microbattery 10 comprises a network of Si nanowires 24 with a diameter of the order of 10 nm, with an empty space rate 26 of 80%, deposited on an insulating substrate 12 on which the current collector 14 b, for example in Pt, has been deposited.
  • the height of the nanotubes 24 or the thickness of the anode 20 is 1 ⁇ m.
  • a 1 ⁇ m layer of electrolyte 18 in LiPON is deposited by radiofrequency sputtering; the cathode 16 then consists of a 3 ⁇ m LiCoO 2 layer, deposited by sputtering or with a magnetron or radiofrequencies, for example.
  • the electrode structure according to the invention generally provides an increase in the conduction properties, required for proper operation of a battery electrode material.
  • the device 10 according to the invention be encapsulated in fine; this encapsulation may occur for an insulated device, or for a set of microbatteries.
  • the encapsulation 22 which has the purpose of protecting the active stack 14 , 16 , 18 , 20 , from the outside environment and specifically from moisture, may be made from ceramic, polymer (such as hexamethyldisiloxane or parylene) or from metal, as well as by a superimposition of layers of these different materials.
  • the electrode structure according to the invention may also be used for the cathode, or even for both electrodes.

Abstract

A new anode configuration (20) is proposed for a lithium microbattery (10). The anode (20) preferably consists of nanotubes or of nanowires (24) such that the empty space (26) left between the different components (24) provides compensation for the inherent swelling upon discharging the microbattery (10). With the absence of stresses on the electrolyte (18), the lifetime of the battery (10) may be increased.

Description

    TECHNICAL FIELD
  • The invention relates to the field of power storage devices, and mainly of microbatteries made in thin films by vacuum deposition methods.
  • More particularly, the invention relates to an electrode for a battery, notably a lithium battery, the structure of which is defined so as to optimize reliability of power storage.
    • STATE OF THE PRIOR ART
  • Among power storage devices, microbatteries which are particularly used, so-called <<fully solid>>batteries, are in the form of films: all the components of the microbattery, i.e., the current collectors, the positive and negative electrodes, the electrolyte and even the encapsulation, are thin layers, obtained by deposition, mainly by physical vapor deposition (PVD) or chemical vapor deposition (CVD). The techniques used allow objects to be made with any shapes.
  • As usual, the operating principle of such a battery is based on the insertion and removal, also called <<disinsertion>>, of an alkaline metal ion or a proton into and from the positive electrode, and the deposition or extraction of this ion on and from the negative electrode. According to the materials used, the operating voltage of this type of battery is between 1 and 4 V, and the surface capacities are of the order of a few 10 μAh/cm2 to a few hundreds of μAh/cm2. Recharging a microbattery, i.e., transferring ions from the anode to the cathode is generally complete after a few minutes of charging.
  • Main systems use Li+ as a ion species for transporting the current: the Li+ ion extracted from the cathode during the discharge of the battery will be deposited on the anode, and vice versa, it will be extracted from the anode in order to be inserted in the cathode during the charging. However, the melting point of lithium, 181° C., limits potential use of the battery for high temperatures; in particular, it is impossible to carry out a solder reflow process of the different material layers. Moreover, the strong reactivity of lithium metal with regard to the ambient atmosphere is a penalty, even for the encapsulation. Finally, it is impossible to spray lithium metal, so it is necessary to perform thermal evaporation.
  • Another option is to select an anode made from a material for inserting the Li+ ion (Li-ion battery), which comes from a cathode, the material of which contains lithium. Now, insertion of the Li+ ion causes swelling of the material which receives it: even the most performing materials used as insertion anodes, such as Si, lead to significant volume expansions (up to 400%). The stresses generated by such a difference in volume strongly strain the superimposed layers, and in particular may cause deteriorations, or even cracks, of the juxtaposed electrolyte, which may create short-circuits making the battery inoperative.
  • Another alternative is the anodeless battery (also known as a Li-free battery): depositing of Li+ from the cathode is directly carried out on a substrate, a so-called blocking substrate. The protrusions generated by the deposition however are also the source of strong deformations and of potential breaking of the electrolyte.
  • Problems of stresses in Li-ion or Li-free microbatteries lead to short-circuit rates of the order of 90% after 1000 charging/discharging cycles (versus 5% for lithium metal anodes).
  • These problems are naturally not posed in batteries with a liquid electrolyte or gel electrolyte, which may be dispersed between the electrodes, and examples of which are given in WO 99/65821.
  • For fully solid batteries, it was of course suggested that the electrolyte be changed so as to make it in several portions, by inserting inside it fine layers of another material, also a lithium ion conductor, in order to limit possible diffusion of cracks right through the electrolyte layer (see for example U.S. Pat. No. 6,770,176). Such a solution however results in multiplying the number of layers to be deposited (with at least two different targets for the electrolyte), which increases the cost of the manufacturing method, and may only degrade the ionic conductivity of the electrolyte.
    • DISCUSSION OF THE INVENTION
  • The object of the invention is to overcome the problems of the state of the art as for the stability of the power storage and supply. More particularly, the invention recommends the use of a new family of electrodes, the architecture and design of which provide suppression of the stresses on the electrolyte during the charging and discharging of the microbattery.
  • In particular, the expansion of the anode in the direction perpendicular to the substrate and to the electrolyte layer is suppressed.
  • In one aspect, the invention relates to a microbattery, an electrode of which is formed by independent electrode components, which thereby define gaps without any electrode between them, or empty spaces. Preferably, the empty space rate is larger than 50%, for example of the order of 80%.
  • The relevant electrode is mainly the anode, the cathode and the solid electrolyte then being in the form of material layers, deposited more or less uniformly. Preferably the anode consists of protrusions extending and protruding from a current-collecting substrate. In particular, for a lithium microbattery, the anode consists of carbon nanotubes or silicon nanowires. Thus, the solid electrolyte rests on the free end of the anode components or more generally the electrolyte layer is held above cavities present between the components of the relevant electrode.
  • The power storage device according to the invention may be encapsulated in order to insulate the ion exchanger components from the outside.
  • According to another aspect, the invention relates to a nanowire or nanotube structure on a conducting substrate which may be used for making lithium batteries, as an electrode.
    • SHORT DESCRIPTION OF THE DRAWINGS
  • The features and advantages of the invention will be better understood upon reading the description which follows and with reference to the appended drawings, given as an illustration and by no means limiting.
  • FIG. 1 schematically illustrates power storage according to the invention.
  • FIGS. 2A and 2B show a device according to the invention in the charged condition and in the discharged condition, respectively.
    • DETAILED DISCUSSION OF PARTICULAR EMBODIMENTS
  • As schematized in FIG. 1, a power storage device usually comprises a substrate 12, cathode 14 a and anode 14 b collectors (the latter may be integral with the substrate 12), a cathode 16, an electrolyte 18, and an anode 20. Moreover, the microbattery 10 may be protected by an encapsulation layer 22: the electrodes 16, 20, notably when they are in lithium, are indeed very reactive towards air, and it may be advantageous to also encapsulate the other components 14, 18.
  • The total thickness of the stack 14, 16, 18, 20 is usually between 10 and 50 μm, advantageously of the order of 15 μm. Such a microbattery 10, except for the anode 20 which will be described later on, may be made by any known technique, and in particular with different materials:
  • The current collectors 14 are metal and may for example be deposits based on Pt, Cr, Au, Ti.
  • The positive electrode 16 may notably consist of LiCoO2, LiNiO2, LiMn2O4, CuS, CuS2, WOySz, TiOySz, V2O5, deposited by a standard technique, with possible thermal annealing in order to increase crystallization and insertion capabilities (notably for lithiated oxides).
  • The electrolyte 18, which is a good ionic conductor and an electronic insulator, generally consists of a glassy material based on boron oxide, on lithium salts or oxides, in particular a lithium oxynitride. Preferably the electrolyte is based on a phosphate, such as LiPON, or LiSiPON.
  • In a device 10 according to the invention and as illustrated in FIG. 1, the anode 20 is however made according to an architecture with which any expansion in the direction perpendicular to the surface of the collector substrate 14 b and at the adjacent electrolyte surface 18 may be suppressed. This advantage is obtained by means of an electrode 20 comprising electrode components 24 spaced apart from each other, and therefore an anode 20 comprising empty spaces 26: during discharge of the cathode 16, lithium ions will cause swelling of the anode components 24, but the expansion is achieved in the residual empty space 26. Consequently, the electrolyte 18, held by the free ends of the anode components 24, no longer undergoes any induced stress during charging and discharging. Further, this empty space also allows Li+ ions which are not inserted in the anode, to be received and which are deposited as lithium metal. Unlike the close geometry described in WO 99/65821, the electrolyte 18, as a layer, is not at all strained by the expansion because, contrary to a liquid or a gel, the electrolyte 18 does not fit into the residual empty space 26.
  • Advantageously, the initially present empty space proportion 26 compensates the increase in volume related to the insertion of lithium in the components 24. This optimization is specific to each insertion material, but the empty space rate is usually larger than 50%, preferably larger than 80%.
  • An example is schematized in FIG. 2: FIG. 2A illustrates the charged condition of the battery 10, in which the anode 20 does not comprise any Li+ ions. During charging, the lithium ions will be inserted into the anode components 24 causing them to swell, so that the residual empty space 26 decreases. However, even in the totally discharged condition of the battery, as schematized in FIG. 2B, the overall volume of the anode layer 20 has not changed, only the empty space rate 26 has decreased, so that neither the electrolyte 18 nor the collector layer 14 b have undergone any stress.
  • The materials used for making the protrusions 24 are materials into which lithium may be inserted (a preferred empty space rate is shown between brackets): germanium (80%), silicon-germanium (80%), silver, tin (70%), . . . and especially silicon (80%) or carbon (50%).
  • The use of nanostructures, i.e., with sectional dimensions less than a few tens of nanometers, in particular nanotubes and nanowires, is recommended in obtaining optimal results for the expansion problems. In particular, in the case of electrode components 24 as nanotubes, an additional advantage resides in the fact that with the growth of these nanotubes, it is possible to do without the photolithographic step, a very difficult step because of the required precision.
  • Any technology with which structures of this type (a diameter with very small dimensions) may be obtained, may be used such as full layer deposition followed by the definition of small patterns by photolithography. As for deposition of nanotubes or nanofibers, techniques are described for example in the documents of Sharma S and al.: <<Diameter control of Ti-catalyzed silicon nanowires>>, J. Crystal Growth 2004; 267: pp. 613-618, or Tang H and al.: <<High dispersion and electrocatalytic properties of platinum on well-aligned carbon nanotube arrays>>, Carbon 2004; 42: pp. 191-197.
  • The electrode components 24 may be randomly positioned forming a sponge type network. Preferably, the components of electrodes are in the form of protrusions 24 protruding from the surface of the collector substrate 14 b, in particular as a regular network, for example a square or hexagonal network. The diameter of the protrusions 24 and the pitch of the network may be optimized in order to obtain the sought-after-empty space rate.
  • In particular, growth of nanowires or nanotubes is preferred, and the obtained network may be regular, with notably protrusions 24 which all protrude from the base surface 14 b, according to an angle advantageously as close as possible to 90°. The protrusions 24 may thus consist in a network of wires with a diameter from 5 to 50 nm, spaced apart by 50 to 100 nm with heights between 200 nm and 5 μm.
  • For example, a microbattery 10 according to the invention comprises a network of Si nanowires 24 with a diameter of the order of 10 nm, with an empty space rate 26 of 80%, deposited on an insulating substrate 12 on which the current collector 14 b, for example in Pt, has been deposited. The height of the nanotubes 24 or the thickness of the anode 20 is 1 μm. Next, a 1 μm layer of electrolyte 18 in LiPON is deposited by radiofrequency sputtering; the cathode 16 then consists of a 3 μm LiCoO2 layer, deposited by sputtering or with a magnetron or radiofrequencies, for example.
  • In addition to the advantage of avoiding any swelling of the anode 20, the electrode structure according to the invention generally provides an increase in the conduction properties, required for proper operation of a battery electrode material.
  • Moreover, it is preferable that the device 10 according to the invention be encapsulated in fine; this encapsulation may occur for an insulated device, or for a set of microbatteries. The encapsulation 22, which has the purpose of protecting the active stack 14, 16, 18, 20, from the outside environment and specifically from moisture, may be made from ceramic, polymer (such as hexamethyldisiloxane or parylene) or from metal, as well as by a superimposition of layers of these different materials.
  • It should be further noted that, by means of the invention, encapsulation is facilitated, the layer of which, as the one of the electrolyte, is sensitive to problems of stresses and deformation:
  • no change in volume of the device 10 occurs,
  • by not using lithium metal, it is possible to generate a less chemically sensitive electrode material and a more smooth surface, on which the encapsulation layers 22 are deposited.
  • Although described for the anode, it is clear that the electrode structure according to the invention may also be used for the cathode, or even for both electrodes.
  • Among the targeted applications, supplying power to microsystems appears, in addition to chip cards and smart labels, with which recurrent measurement of parameters may be conducted by miniaturized implants. These applications impose that all the layers required for operating the battery should be made with techniques compatible with industrial methods of microelectronics, which is the case of the device according to the invention.

Claims (17)

1. A power storage device comprising at least one first electrode, consisting of a plurality of electrode components defining gaps between them, a second electrode and an electrolyte t localized between both electrodes, characterized in that the electrolyte is solid, and held above the gaps by electrode components.
2. The device according to claim 1, wherein the volume occupied by the electrode components is less than 50%, preferably of the order of 20% of the volume defined by the first electrode.
3. The device according to claim 1, wherein the first electrode is positioned on a surface of a collector substrate.
4. The device according to claim 3, wherein the electrode components form a network of protrusions which protrude from the surface of the collector substrate.
5. The device according to claim 4, wherein the protrusions have a surface included in a circle with a diameter between 5 and 50 nm and are spaced apart by 50 to 100 nm.
6. The device according to claim 4, wherein the protrusions extend over 200 nm to 5 μm perpendicularly to the surface of the collector substrate.
7. The device according to claim 1, wherein the first electrode is the anode.
8. The device according to claim 7, wherein the electrode components are carbon or silicon nanotubes or nanowires.
9. The device according to claim 1, wherein the second electrode and the electrolyte each consist of a material layer.
10. The device according to claim 1 which is a lithium microbattery.
11. The device according to claim 10, wherein the electrolyte is a lithium oxynitride.
12. The device according to claim 1, further comprising an encapsulation layer which insulates the electrodes and the electrolyte from the outside environment.
13. The use of a component consisting of nanowires or nanotubes on an electrically conducting substrate in the making of a lithium battery electrode, for which the electrolyte is solid and in the form of a layer.
14. The device according to claim 2, wherein the first electrode is positioned on a surface of a collector substrate.
15. The device according to claim 5, wherein the protrusions extend over 200 nm to 5 μm perpendicularly to the surface of the collector substrate.
16. The device according to claim 6, wherein the first electrode is the anode.
17. The device according to claim 8, wherein the second electrode and the electrolyte each consist of a material layer.
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